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https://hdl.handle.net/11499/9457
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DC Field | Value | Language |
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dc.contributor.author | Özturk, Önder | - |
dc.contributor.author | Başay, Bürge Kabukçu | - |
dc.contributor.author | Büber, Ahmet | - |
dc.contributor.author | Başay, Ömer | - |
dc.contributor.author | Alaçam, Hüseyin | - |
dc.contributor.author | Bacanli, A. | - |
dc.contributor.author | Yilmaz, Ş.G. | - |
dc.date.accessioned | 2019-08-16T13:01:39Z | |
dc.date.available | 2019-08-16T13:01:39Z | |
dc.date.issued | 2016 | - |
dc.identifier.issn | 1738-3684 | - |
dc.identifier.uri | https://hdl.handle.net/11499/9457 | - |
dc.identifier.uri | https://doi.org/10.4306/pi.2016.13.5.518 | - |
dc.description.abstract | Objective Attention-deficit hyperactivity disorder (ADHD) is a neurodevelopmental disorder that negatively affects different areas of life. We aimed to evaluate the associations between the Val66Met polymorphism of brain-derived neurotrophic factor (BDNF) and ADHD and to assess the effect of the BDNF polymorphism on the neurocognitive profile and clinical symptomatology in ADHD. Methods Two hundred one ADHD cases and 99 typically developing subjects (TD) between the ages of 8 and 15 years were involved in the study. All subjects were evaluated using a complete neuropsychological battery, Child Behavior Checklist, the Teacher’s Report Form (TRF) and the DSM-IV Disruptive Behavior Disorders Rating Scale-teacher and parent forms. Results The GG genotype was significantly more frequent in the patients with ADHD than in the TD controls, and the GG genotype was also significantly more frequent in the ADHD-combined (ADHD-C) subtype patients than in the TDs. However, there were no significant associations of the BDNF polymorphism with the ADHD subtypes or neurocognitive profiles of the patients. The teacher-assessed hyperactivity and inattention symptom count and the total score were higher, and the appropriately behaving subtest score of the TRF was lower in the GG genotypes than in the GA and AA (i.e., the A-containing) genotypes. Conclusion We found a positive association between the BDNF gene Val66Met polymorphism and ADHD, and this association was observed specifically in the ADHD-C subtype and not the ADHD-predominantly inattentive subtype. Our findings support that the Val66Met polymorphism of BDNF gene might be involved in the pathogenesis of ADHD. Furthermore Val66Met polymorphism of BDNF gene may be more closely associated with hyperactivity rather than inattention. © 2016 Korean Neuropsychiatric Association. | en_US |
dc.language.iso | en | en_US |
dc.publisher | Korean Neuropsychiatric Association | en_US |
dc.relation.ispartof | Psychiatry Investigation | en_US |
dc.rights | info:eu-repo/semantics/openAccess | en_US |
dc.subject | Attention-deficit hyperactivity disorder | en_US |
dc.subject | Brain-derived neurotrophic factor | en_US |
dc.subject | Gene polymorphism | en_US |
dc.subject | brain derived neurotrophic factor | en_US |
dc.subject | adolescent | en_US |
dc.subject | adult | en_US |
dc.subject | analysis of variance | en_US |
dc.subject | Article | en_US |
dc.subject | attention deficit disorder | en_US |
dc.subject | child | en_US |
dc.subject | Child Behavior Checklist | en_US |
dc.subject | child psychiatry | en_US |
dc.subject | controlled study | en_US |
dc.subject | DNA extraction | en_US |
dc.subject | DNA polymorphism | en_US |
dc.subject | female | en_US |
dc.subject | genotype phenotype correlation | en_US |
dc.subject | human | en_US |
dc.subject | interview | en_US |
dc.subject | major clinical study | en_US |
dc.subject | male | en_US |
dc.subject | neuropsychological battery | en_US |
dc.subject | neuropsychological test | en_US |
dc.subject | performance | en_US |
dc.subject | risk factor | en_US |
dc.subject | school child | en_US |
dc.subject | scoring system | en_US |
dc.subject | young adult | en_US |
dc.title | Brain-derived neurotrophic factor gene val66met polymorphism is a risk factor for attention-deficit hyperactivity disorder in a Turkish sample | en_US |
dc.type | Article | en_US |
dc.identifier.volume | 13 | en_US |
dc.identifier.issue | 5 | en_US |
dc.identifier.startpage | 518 | |
dc.identifier.startpage | 518 | en_US |
dc.identifier.endpage | 525 | en_US |
dc.identifier.doi | 10.4306/pi.2016.13.5.518 | - |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.identifier.pmid | 27757130 | en_US |
dc.identifier.scopus | 2-s2.0-84991497765 | en_US |
dc.identifier.wos | WOS:000384842300007 | en_US |
dc.identifier.scopusquality | Q2 | - |
dc.owner | Pamukkale University | - |
item.openairecristype | http://purl.org/coar/resource_type/c_18cf | - |
item.openairetype | Article | - |
item.cerifentitytype | Publications | - |
item.fulltext | With Fulltext | - |
item.grantfulltext | open | - |
item.languageiso639-1 | en | - |
crisitem.author.dept | 14.02. Internal Medicine | - |
crisitem.author.dept | 14.02. Internal Medicine | - |
crisitem.author.dept | 14.02. Internal Medicine | - |
Appears in Collections: | PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection Tıp Fakültesi Koleksiyonu WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection |
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